Author

B. Alobaidi

Newcastle UniversityORCID 0000-0003-2718-4826Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Giles S. HoltiD· 2 shared Joris Andre VeltmaniD· 2 shared Liliana RamosiD· 2 shared Lois E. Batty· 2 shared Manon S. OudiD· 2 shared Miguel Joao XavieriD· 2 shared Alberto BarrosiD· 1 shared Alexandra Manuel LopesiD· 1 shared

Activity by Year

2022-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Giles S. HoltORCID

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2 papers

Recent·Most cited

GenomicsHuman MutationPeer-reviewedSep 1, 2022

Phasing of de novo mutations using a scaled-up multiple amplicon long-read sequencing approach

Giles S. Holt, Lois E. Batty, B. Alobaidi…·Joris Andre Veltman

This study phases de novo mutations using a combined long-read and short-read sequencing approach, successfully determining parent-of-origin for 71% of analyzed mutations.

8 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GeneticsNature CommunicationsPeer-reviewedJan 10, 2022

A de novo paradigm for male infertility

Manon S. Oud, RM Smits, H E Smith…·Joris Andre Veltman

The paper identifies de novo mutations as a significant genetic cause of male infertility, finding several candidate genes and an enrichment of loss-of-function and missense mutations in intolerant genes.

98 citationstop 1%

humanwhole-exome sequencing

𝕏 PostBluesky